is an important predictor of refractoriness to chemotherapy and poor survival in intermediate-risk acute myeloid leukemia (AML)
Résumé
We have analyzed brain and acute leukemia, cytoplasmic () gene expression and other genetic markers (, , , , , , and mutations) in 127 intermediate-risk acute myeloid leukemia (AML) patients: 98 cytogenetically normal and 29 with intermediate-risk cytogenetic alterations. High versus low expressers showed a higher refractoriness to induction treatment (31% vs 10%; = .005), lower complete remission rate after salvage therapy (82% vs 97%; = .010), and lower 3-year overall (23% vs 58%, < .001) and relapse-free survival (26% vs 52%, = .006). Similar results were found when cytogenetic subgroups were analyzed separately. Multivariate models confirmed the unfavorable prognosis of this marker. In conclusion, is a relevant prognostic marker in intermediate-risk AML.
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